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首页> 外文期刊>Obstetrics and Gynecology: Journal of the American College of Obstetricians and Gynecologists >Surgical staples compared with subcuticular suture for skin closure after cesarean delivery: A randomized controlled trial
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Surgical staples compared with subcuticular suture for skin closure after cesarean delivery: A randomized controlled trial

机译:与剖腹产后皮肤闭合的皮肤缝合术相比:随机对照试验

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OBJECTIVE: To compare the risk of cesarean wound disruption or infection after closure with surgical staples compared with subcuticular suture. METHODS: Women with viable pregnancies at 24 weeks of gestation or greater undergoing scheduled or unscheduled cesarean delivery were randomized to wound closure with surgical staples or absorbable suture. Staples were removed at postoperative days 3-4 for low transverse incisions and days 7-10 for vertical incisions. Standardized wound evaluations were performed at discharge (days 3-4) and 4-6 weeks postoperatively. The primary outcome was a composite of wound disruption or infection within 4-6 weeks. Secondary outcomes included operative time, highest pain score on analog scale, cosmesis score, and patient scar satisfaction score. Analyses were by intent to treat. RESULTS: Of 398 patients, 198 were randomized to staples and 200 to suture (but four received staples). Baseline characteristics including body mass index, prior cesarean delivery, labor, and type of skin incision were similar by group. The primary outcome incidence at hospital discharge was 7.1% for staples and 0.5% for suture (P<.001, relative risk 14.1, 95% confidence interval [CI] 1.9-106). Of 350 (87.9%) with follow-up at 4-6 weeks, the cumulative risk of the primary outcome at 4-6 weeks was 14.5% for staples and 5.9% for suture (P=.008, relative risk 2.5, 95% CI 1.2-5.0). Operative time was longer with suture closure (median time of 58 versus 48 minutes; P<.001). Pain scores at 72-96 hours and at 6 weeks, cosmesis score, and patient satisfaction score did not differ by group. CONCLUSION: Staples closure compared with suture is associated with significantly increased composite wound morbidity after cesarean delivery. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov, www.clinicaltrials.gov, NCT01008449. LEVEL OF EVIDENCE: I
机译:目的:比较与外科钉闭合后剖腹产后剖腹产破坏或感染的风险。方法:在妊娠或更高的妊娠或更高的经历预定或未划分的剖宫产后24周妊娠的妇女随机分配给伤口闭合,用手术表或可吸收的缝合。在术后时间3-4术后拆除术术,用于低横切切口和用于垂直切口的第7-10天。标准化伤口评估在术后在排出时进行(第3-4天)和4-6周。主要结果是在4-6周内伤口破坏或感染的复合物。二次结果包括术术时间,模拟规模的最高疼痛评分,患者瘢痕满意度得分。分析是意图治疗。结果:398例患者,198例随机地与缝合钉和200例(但是四个接受的钉书针)。基线特征在内的体重指数,先前的剖宫产,劳动力和皮肤切口类型是相似的。梭形的前期出院的主要结果发病率为7.1%,缝合线0.5%(P <.001,相对风险14.1,95%置信区间[CI] 1.9-106)。 350(87.9%)随访4-6周,梭形占初级结果的累积风险为梭形为14.5%,缝合线5.9%(P = .008,相对风险2.5,95% CI 1.2-5.0)。缝合闭合的手术时间更长(58的中位时间与48分钟; p <.001)。疼痛分数在72-96小时,6周,患者评分,患者满意度得分没有差异。结论:与缝合线相比的钉闭扣与剖宫产后的复合伤口发病率显着增加。临床试验登记:ClinicalTrials.gov,www.clinicaltrials.gov,NCT01008449。证据水平:我

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